Evidence map›Paper›PMID 30842776›Full record

ArticleFrontiers in immunology2019

Reprogrammed CD4

Roland W Herzog, Veronica Kuteyeva, Rania Saboungi, Cox Terhorst, Moanaro Biswas

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. 3-in-oneiScience · 2025
    Article
  3. Article
  4. The curious case of AAV immunology.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  5. Review
  6. Article
  7. Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. CAR- and TRuC-redirected regulatory T cells differ in capacity to control adaptive immunity to FVIII.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  13. Immunogenicity Challenges Associated with Subcutaneous Delivery of Therapeutic Proteins.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
    Review
  14. Review
  15. Article
  16. Escape or Fight: Inhibitors in Hemophilia A.Frontiers in immunology · 2020
    Review
  17. Review
  18. Review
  19. Review
  20. Tolerating Factor VIII: Recent Progress.Frontiers in immunology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Roland W HerzogHerman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, United States.
Veronica KuteyevaDepartment of Pediatrics, College of Medicine, University of Florida, Gainesville, FL, United States.
Rania SaboungiDepartment of Pediatrics, College of Medicine, University of Florida, Gainesville, FL, United States.
Cox TerhorstDivision of Immunology, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, MA, United States.
Moanaro BiswasHerman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, United States.
University of Florida · USHarvard University · USIndiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Enhancing immune regulation in gene therapy for hemophiliaR01HL131093 · NHLBI · UNIVERSITY OF FLORIDA · PI Ype Peter De Jong, Roland W. Herzog · 2016 to 2026
$7.2M
Skills DevelopmentU54HL142012 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CAMIRE, RODNEY M · 2018 to 2022
$7.0M
Immunology of Factor IX Gene Transfer to LiverR01AI051390 · NIAID · UNIVERSITY OF FLORIDA · PI HERZOG, ROLAND W. · 2002 to 2022
$6.7M
NHLBI NIH HHS R01 HL131093NHLBI NIH HHS U54 HL142012NIAID NIH HHS R01 AI051390
6 · The paper itself

Abstract

Coagulation Factor VIII (FVIII) replacement therapy in hemophilia A patients is complicated by the development of inhibitory antibodies, which often render the treatment ineffective. Previous studies demonstrated a strong correlation between induction of regulatory T cells (Treg) and tolerance to the therapeutic protein. We, therefore, set out to evaluate whether the adoptive transfer of FVIII-specific CD4

Indexed as

Adoptive TransferAnimalsAntibodies, BlockingAntibody FormationB-LymphocytesCD4-Positive T-LymphocytesFactor VIIIForkhead Transcription FactorsHemophilia AImmune ToleranceMaleMiceMice, Inbred BALB CT-Lymphocytes, RegulatoryAntibodies, BlockingFactor VIIIForkhead Transcription FactorsFoxp3 protein, mousecell therapyFoxP3hemophilia Aimmunotherapytolerancetreg

Identifiers

PMID30842776
PMCPMC6391332
OpenAlexW2915355581

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.